A Case of Congenital Aniridia and Familial Pheochromocytoma—With Special Reference to Aniridia-Wilms' Tumor Syndrome

Japanese journal of human genetics
doi 10.1007/bf01900445
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Springer Science and Business Media LLC

Related search

Congenital Aniridia With Cataract: Case Series

BMC Ophthalmology
MedicineOphthalmology
2017English

G and R Banding of 11p Deletions in Aniridia--Wilms' Tumour.

Journal of Medical Genetics
Genetics
1987English

The Genetic Architecture of Aniridia and Gillespie Syndrome

Human Genetics
Genetics
2018English

Aniridia-Renal Agenesis-Psychomotor Retardation Syndrome

2020English

Genetic Approaches to Differential Diagnosis of Hereditary Forms of Congenital Aniridia

Vestnik Rossiiskoi Akademii Meditsinskikh Nauk
Medicine
2017English

Progressive Changes in the Angle in Congenital Aniridia, With Development of Glaucoma

American Journal of Ophthalmology
Ophthalmology
1974English

Aniridia and Wilms's Tumour (Nephroblastoma).

British Journal of Ophthalmology
Molecular NeuroscienceOphthalmologySensory SystemsCellular
1968English

Inherited KIF21A and PAX6 Gene Mutations in a Boy With Congenital Fibrosis of Extraocular Muscles and Aniridia

BMC Medical Genetics
Genetics
2013English

PAX6 Gene Analysis in Serbian Patients With Aniridia

Medicinski podmladak
2016English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2025 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy